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"70518-2115-1" National Drug Code (NDC)

Prednisone 21 TABLET in 1 BLISTER PACK (70518-2115-1)
(REMEDYREPACK INC.)

NDC Code70518-2115-1
Package Description21 TABLET in 1 BLISTER PACK (70518-2115-1)
Product NDC70518-2115
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePrednisone
Non-Proprietary NamePrednisone
Dosage FormTABLET
UsageORAL
Start Marketing Date20190523
Marketing Category NameANDA
Application NumberANDA088832
ManufacturerREMEDYREPACK INC.
Substance NamePREDNISONE
Strength10
Strength Unitmg/1
Pharmacy ClassesCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2115-1





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